ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.*2771_*2775del

dbSNP: rs35656864
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000345628 SCV000406156 uncertain significance Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000391436 SCV000406157 uncertain significance Andersen Tawil syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000306146 SCV000406158 uncertain significance Short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694363 SCV005193052 uncertain significance not provided criteria provided, single submitter not provided

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